The origin of the chemical composition of ethylene/propylene copolymer produced with Ziegler–Natta catalysts is investigated in terms of the active site nature and transient monomer concentration during polymerization. Using various catalysts including TiCl3/MgCl2 model catalysts with controlled Ti dispersion and TiCl4/internal donor/MgCl2 traditional catalysts, normal‐pressure and pressurized slurry copolymerization is conducted at various ethylene/propylene feed ratios. This study finds that the copolymer composition strongly depends on the copolymerization yield rather than the active site nature for both of the normal‐pressure and pressurized copolymerization. The ethylene concentration becomes smaller than its equilibrium concentration during copolymerization primarily due to the great activity enhancement in the copolymerization and secondarily due to the high reactivity and low solubility of ethylene. It is shown that the decrease in the ethylene concentration during copolymerization causes the variation of the copolymer composition in a way dependent on the kinetic profile of employed catalysts, thus broadening the chemical composition distribution.